methyl-4-{3-(3-hydroxy-(1E)-pentenyl)-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylaminocarbonyl}butanoate

Base Information

Chemical Name:methyl-4-{3-(3-hydroxy-(1E)-pentenyl)-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylaminocarbonyl}butanoate
CAS No.:197707-62-3
Molecular Formula:C₂₈H₃₅NO₆
Molecular Weight:481.589
Hs Code.:

Synonyms:methyl-4-{3-(3-hydroxy-(1E)-pentenyl)-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylaminocarbonyl}butanoate

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Chemical Property of methyl-4-{3-(3-hydroxy-(1E)-pentenyl)-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylaminocarbonyl}butanoate

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Technology Process of methyl-4-{3-(3-hydroxy-(1E)-pentenyl)-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylaminocarbonyl}butanoate

There total 13 articles about methyl-4-{3-(3-hydroxy-(1E)-pentenyl)-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylaminocarbonyl}butanoate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 502-44-3,24980-41-4,80137-66-2
hexahydro-2H-oxepin-2-one

: 197707-62-3
methyl-4-{3-(3-hydroxy-(1E)-pentenyl)-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylaminocarbonyl}butanoate

Guidance literature:: Multi-step reaction with 7 steps

1: conc. sulfuric acid / 1 h / Heating

2: AlCl₃ / 1,2-dichloro-ethane / 2.5 h / 15 °C

3: 5N aq. NaOH / methanol / 1 h / 25 °C

4: NaBH₄ / methanol / 1 h / 25 - 65 °C

5: 73 percent / KCl / dimethylsulfoxide / 4 h / 170 °C

6: 92 percent / triethylamine / CH₂Cl₂ / 1 h

7: 1.) NaH / 1.) DMF, a) from 0 deg C to 25 deg C, b) 25 deg C, 30 min, 2.) DMF, 60 deg C, 2 h

With sodium hydroxide; sodium tetrahydroborate; aluminium trichloride; sulfuric acid; potassium chloride; sodium hydride; triethylamine; In methanol; dichloromethane; dimethyl sulfoxide; 1,2-dichloro-ethane;
DOI:10.1016/S0968-0896(97)00089-8

Reference yield:

: 1501-26-4
methyl 4-(chlorocarbonyl)butyrate

: 197707-62-3
methyl-4-{3-(3-hydroxy-(1E)-pentenyl)-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylaminocarbonyl}butanoate

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) pyridine, 2.) 1N aq. HCl / 1.) CH₂Cl₂, 25 deg C, 15 min

2: 100 percent / CH₂Cl₂ / 2 h / 25 °C

3: 71 percent / NaBH₄ / tetrahydrofuran; methanol / 0.33 h / 0 °C

4: 1.) NaH / 1.) DMF, a) from 0 deg C to 25 deg C, b) 25 deg C, 30 min, 2.) DMF, 60 deg C, 2 h

With pyridine; hydrogenchloride; sodium tetrahydroborate; sodium hydride; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1016/S0968-0896(97)00089-8

Reference yield:

: 128577-60-6
(5E)-6-(4-Methoxyphenyl)-5-hexen-1-ol

: 197707-62-3
methyl-4-{3-(3-hydroxy-(1E)-pentenyl)-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylaminocarbonyl}butanoate

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / triethylamine / CH₂Cl₂ / 1 h

2: 1.) NaH / 1.) DMF, a) from 0 deg C to 25 deg C, b) 25 deg C, 30 min, 2.) DMF, 60 deg C, 2 h

With sodium hydride; triethylamine; In dichloromethane;
DOI:10.1016/S0968-0896(97)00089-8